TY - JOUR
T1 - Transcriptional interactions suggest niche segregation among microorganisms in the human gut
AU - Plichta, Damian Rafal
AU - Juncker, Agnieszka Sierakowska
AU - Bertalan, Marcelo
AU - Rettedal, Elizabeth
AU - Gautier, Laurent
AU - Varela, Encarna
AU - Manichanh, Chaysavanh
AU - Fouqueray, Charlène
AU - Levenez, Florence
AU - Nielsen, Trine
AU - Doré, Joël
AU - Machado, Ana Manuel Dantas
AU - de Evgrafov, Mari Cristina Rodriguez
AU - Hansen, Torben
AU - Jørgensen, Torben
AU - Bork, Peer
AU - Guarner, Francisco
AU - Pedersen, Oluf
AU - Metagenomics of the Human Intestinal Tract (MetaHIT) Consortium
AU - Sommer, Morten O A
AU - Ehrlich, S Dusko
AU - Sicheritz-Pontén, Thomas
AU - Brunak, Søren
AU - Nielsen, H Bjørn
PY - 2016/8/26
Y1 - 2016/8/26
N2 - The human gastrointestinal (GI) tract is the habitat for hundreds of microbial species, of which many cannot be cultivated readily, presumably because of the dependencies between species(1). Studies of microbial co-occurrence in the gut have indicated community substructures that may reflect functional and metabolic interactions between cohabiting species(2,3). To move beyond species co-occurrence networks, we systematically identified transcriptional interactions between pairs of coexisting gut microbes using metagenomics and microarray-based metatranscriptomics data from 233 stool samples from Europeans. In 102 significantly interacting species pairs, the transcriptional changes led to a reduced expression of orthologous functions between the coexisting species. Specific species-species transcriptional interactions were enriched for functions important for H2 and CO2 homeostasis, butyrate biosynthesis, ATP-binding cassette (ABC) transporters, flagella assembly and bacterial chemotaxis, as well as for the metabolism of carbohydrates, amino acids and cofactors. The analysis gives the first insight into the microbial community-wide transcriptional interactions, and suggests that the regulation of gene expression plays an important role in species adaptation to coexistence and that niche segregation takes place at the transcriptional level.
AB - The human gastrointestinal (GI) tract is the habitat for hundreds of microbial species, of which many cannot be cultivated readily, presumably because of the dependencies between species(1). Studies of microbial co-occurrence in the gut have indicated community substructures that may reflect functional and metabolic interactions between cohabiting species(2,3). To move beyond species co-occurrence networks, we systematically identified transcriptional interactions between pairs of coexisting gut microbes using metagenomics and microarray-based metatranscriptomics data from 233 stool samples from Europeans. In 102 significantly interacting species pairs, the transcriptional changes led to a reduced expression of orthologous functions between the coexisting species. Specific species-species transcriptional interactions were enriched for functions important for H2 and CO2 homeostasis, butyrate biosynthesis, ATP-binding cassette (ABC) transporters, flagella assembly and bacterial chemotaxis, as well as for the metabolism of carbohydrates, amino acids and cofactors. The analysis gives the first insight into the microbial community-wide transcriptional interactions, and suggests that the regulation of gene expression plays an important role in species adaptation to coexistence and that niche segregation takes place at the transcriptional level.
KW - Journal Article
U2 - 10.1038/nmicrobiol.2016.152
DO - 10.1038/nmicrobiol.2016.152
M3 - Letter
C2 - 27564131
SN - 2058-5276
VL - 1
SP - 1
EP - 6
JO - Nature Microbiology
JF - Nature Microbiology
M1 - 16152
ER -